Canonical Allele Identifier: PA215485
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2630Ile
CA014160
NM_000038.6:c.7888G>A